Development and application of an indirect ELISA for the detection of antibodies to novel duck reovirus

文献类型: 外文期刊

第一作者: Yun, Tao

作者: Yun, Tao;Yu, Bin;Zhang, Cun;Chen, Liu;Ni, Zheng;Hua, Jionggang;Ye, Weicheng;Chen, Haipeng

作者机构:

关键词: Novel duck reovirus (N-DRV);sigma C protein;Indirect ELISA;Serological survey

期刊名称:JOURNAL OF VIROLOGICAL METHODS ( 影响因子:2.014; 五年影响因子:2.001 )

ISSN:

年卷期:

页码:

收录情况: SCI

摘要: A novel duck reovirus (N-DRV) disease emerged in China in 2000 and it has become an epidemic genotype. A test for detection of virus-specific antibodies in serum samples would be useful for epidemiological investigations. Currently, Currently, serological assays for N-DRV diagnosis are not available. A test for detection of virus-specific antibodies in serum samples would be useful for epidemiological investigations. In this study, a highly sensitive and specific indirect enzyme-linked immunosorbent assay (ELISA) for the detection of antibodies to N-DRV was developed. The outer capsid (sigma C) of N-DRV was cloned and expressed in Escherichia coil as a coating antigen. The antigen concentration and serum dilution were optimized using a checkerboard titration. Furthermore, the specificity of sigma C-ELISA assay was confirmed by cross checking with other duck viral pathogens. In comparison with the western blot, the sensitivity and specificity of the sigma C-ELISA was 92.6% and 88.9%, respectively, and agreement of two tests was excellent with kappa value of 0.786 (p < 0.05). A serological survey was performed using the assay on serum samples from different age and species of duck flocks in the Zhejiang and Jiangsu Province, China. The seropositive rate of the 1209 serum samples was 57.7%. In conclusion, the developed sigma C-ELISA assay is a very specific and sensitive test that will be useful for large-scale serological survey in N-DRV infection and monitoring antibodies titers against N-DRV. (C) 2015 Elsevier B.V. All rights reserved.

分类号: R37

  • 相关文献

[1]Prokaryote expression of HPeV-1 VP1 protein, production of VP1 polyclonal antibody and the development of an ELISA. Yu, Ying,Shan, Tongling,Zhu, Caixia,Hua, Xiuguo,Shan, Tongling,Wang, Chunmei,Zhu, Shaofeng,Wang, Chunmei.

[2]Development and application of an indirect enzyme-linked immunosorbent assay based on recombinant capsid protein for the detection of mink circovirus infection. Ge, Junwei,Cui, Xingyang,Shi, Yunjia,Wei, Chengwei,Wen, Shanshan,Xia, Shuang,Zhao, Lili,Chen, Hongyan,Ge, Junwei. 2018

[3]A serological survey of Akabane virus infection in cattle and sheep in northwest China. Qiao Jun,Meng Qingling,Zhang Zaichao,Cai Kuojun,Chen Chuangfu,Qiao Jun,Zhang Jingsheng,Ma Minxing.

[4]Lowly pathogenic avian influenza (H9N2) infection in Plateau pika (Ochotona curzoniae), Qinghai Lake, China. Yu, Zhijun,Zhang, Kun,Qin, Chuan,Xia, Xianzhu,Yu, Zhijun,Zhang, Kun,Qin, Chuan,Xia, Xianzhu,Yu, Zhijun,Cheng, Kaihui,Sun, Weiyang,Xin, Yue,Li, Lin,Huang, Jing,Sang, Xiaoyu,Li, Xue,Wang, Tiecheng,Qian, Jun,Gao, Yuwei,Xia, Xianzhu,Cai, Jinshan,Ma, Ruilin,Zhao, Quanbang,Cheng, Kaihui,Huang, Jing,Li, Xue.

[5]The prevalence of porcine teschovirus in the pig population in northeast of China. Qiu, Zheng,Zhang, Bingkun,Zhang, Jing,Cui, Shangjin,Wang, Zhongtian.

[6]Development and Preliminary Application of an Indirect ELISA to Detect Infectious Bovine Rhinotracheitis Virus Using Recombinant Glycoprotein D of IBRV Strain SD. Song, Lingling,Zhang, Hui,Hou, Peili,Wang, Hongmei,Zhao, Guimin,He, Hongbin,Xia, Xianzhu. 2016

[7]Performance of Indirect ELISA for Maize Hybrid Purity Test. Liu, Yuehui,Wang, Jun,Yang, XinChao,Sun, Naxin,Xu, Lihua. 2013

[8]A novel fusion protein-based indirect enzyme-linked immunosorbent assay for the detection of bovine tuberculosis. Liu, Siguo,Guo, Sheping,Wang, Chunlai,Shao, Meili,Zhang, Xiuhua,Guo, Yang,Gong, Qiang. 2007

[9]An indirect ELISA for detection of Theileria spp. antibodies using a recombinant protein (rTlSP) from Theileria luwenshuni. He, Haining,Li, Youquan,Liu, Junlong,Liu, Zhijie,Yang, Jifei,Liu, Aihong,Chen, Ze,Ren, Qiaoyun,Guan, Guiquan,Liu, Guangyuan,Luo, Jianxun,Yin, Hong,Yin, Hong.

[10]Development of an indirect ELISA for serological detection of reticuloendotheliosis virus using the gp90 protein expressed in Pichia pastoris. Li, Kai,Gao, Honglei,Gao, Li,Qi, Xiaole,Gao, Yulong,Qin, Liting,Wang, Yongqiang,Wang, Xiaomei.

[11]Detection of the Soybean Allergenic Protein Gly m Bd 28K by an Indirect Enzyme-Linked Immunosorbent Assay. Liu, Bin,Teng, Da,Wang, Xiumin,Wang, Jianhua,Liu, Bin,Teng, Da,Wang, Xiumin,Wang, Jianhua.

[12]Development of an Indirect ELISA with Artificially Synthesized N Protein of PPR Virus. Zhu, Yu-min,Dong, Shi-juan,Yu, Rui-song,Li, Zhen,Zhu, Yu-min,Dong, Shi-juan,Yu, Rui-song,Li, Zhen,Zhang, Guo-rui,Lei, Zhi-hai,Zeng, Jiang-yong,Zhu, Se,Duoji, Ciren. 2012

[13]Ducks as a potential reservoir for Pasteurella multocida infection detected using a new rOmpH-based ELISA. Liu, Rongchang,Chen, Cuiteng,Cheng, Longfei,Lu, Ronghui,Fu, Guanghua,Shi, Shaohua,Chen, Hongmei,Wan, Chunhe,Lin, Jiansheng,Fu, Qiuling,Huang, Yu. 2017

[14]Expression of the soybean allergenic protein P34 in Escherichia coli and its indirect ELISA detection method. Liu, Bin,Teng, Da,Wang, Xiumin,Yang, Yalin,Wang, Jianhua,Liu, Bin,Teng, Da,Wang, Xiumin,Yang, Yalin,Wang, Jianhua. 2012

[15]Differential Diagnosis of Antibody to Classical Swine Fever Virus Field Strain by ELISA with Recombinant E2 Proteins of Various Group CSFV. Qiu Chang-Qing,Hu Hui,Cao Xiao-An,Zhou Ji-Zhang,Lin Guo-Zhen,Hu Hui. 2008

[16]Development and application of G(1)-ELISA for detection of antibodies against bovine ephemeral fever virus. Zheng, Fu-ying,Lin, Guo-zhen,Qiu, Chang-qing,Zhou, Ji-zhang,Cao, Xiao-an,Gong, Xiao-wei. 2009

作者其他论文 更多>>